GB1560083A - Detergent compositions - Google Patents

Detergent compositions Download PDF

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GB1560083A
GB1560083A GB5351976A GB5351976A GB1560083A GB 1560083 A GB1560083 A GB 1560083A GB 5351976 A GB5351976 A GB 5351976A GB 5351976 A GB5351976 A GB 5351976A GB 1560083 A GB1560083 A GB 1560083A
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composition according
alkyl
ethylene oxide
nonionic surfactant
surfactant
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Procter and Gamble Co
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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/825Mixtures of compounds all of which are non-ionic
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/722Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele groups

Description

(54) DETERGENT COMPOSITIONS (71) We, THE PROCTER & GAMBLE COMPANY, a Corporation organised and existing under the laws of the State of Ohio, United States of America, of 301 East Sixth Street, Cincinnati, Ohio 45202, United States of America, do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement: This invention relates to detergent compositions and, in particular, to detergent compositions which comprise, in combination, an alkyl glyceryl ether and an ethoxylated non-ionic surfactant.
Conventional detergent compositions have adequate cleaning performance in most situations. However, one major problem area which remains is the removal of greasy and oily materials from fabrics. This problem is particularly pronounced with certain of the newer synthetic fabrics and is also particularly serious in the case of hydrocarbon-based oils such as used motor oil. There is therefore a clear need to improve the performance of detergent compositions in terms of grease and oil removal.
It has been recognized that nonionic surfactants can offer certain advantages in this area, and the incorporation of surfactants such as ethoxylated alcohols into detergent compositions does provide some benefit in oily stain removal. Unfortunately, this benefit does not extend to a wide spectrum of fabric/oily stain combinations and, in particular, removal of hydrocarbon oil stain, especially on cotton, tends to be difficult.
It is an object of the present invention to provide a particular combination of surfactant materials which offers improved performance on oily stain removal through the wash.
Description of the Prior Art Alkyl glyceryl ethers are known material and various uses have been suggested for them.
For example, they have been suggested as fixing agents for perfumes in US Patent No.
2,091,162; as superfatting agents in soap in US Patent No. 2,157,022; and as extracting agents for organic substances in US Patent No. 2,156,724.
Furthermore, these and related materials have been suggested for use in detergent compositions for certain purposes. US Patent No. 2,768, 956, issued October 30, 1956 to Scott, discloses acylaryl glyceryl ethers in detergent compositions containing ionic non-soap surfactants. The glyceryl ethers in this case are said to be suds stabilizers. US Patent No. 2,900,246, issued August 18, 1959 to Fowkes and Sawyer, also discloses the utility of glyceryl ethers as foam stabilizers for ionic, particularly sulfate and sulfonate, surfactants. US Patent No.
3,427,248, issued February 11, 1969 to Lamberti et al, discloses the use of certain higher alkyl polyol ethers in combination with detergents as suds boosters and lime scum dispersants.
The utilization of naturally-occurring glyceryl ethers such as selachyl alcohol and batyl alcohol is discussed by M. Sulzbacher in Manufacturing Chemist, 1962, 33, 232 and it is suggested that these materials could have surface activity and could be made watercompatible by ethoxylation of the hydroxyl groups.
West German Offenlegungsschrift 2,657,518 relates to certain novel glyceryl ethers of ethoxylated alcohols which are themselves surfactants and are useful in detergent compositions.
None of the above discussed art references have recognized the particularly beneficial effect on greasy and oily soil removal obtained by using compositions of the present invention comprising a combination of an alkyl glyceryl ether and a specific type of nonionic surfactant.
Summary of the Invention According to the invention, there is provided a detergent composition comprising a combination consisting of (a) from 80% to 20% by weight of monoglyceryl ether of the general formula
wherein R is a substantially linear alkyl or alkenyl moiety having from 8 to 16 carbon atoms, and (b) from 20%to 80%by weight of a nonionic surfactant which is a condensation product of a Cs-C15 alcohol with an alkylene oxide selected from ethylene oxide and mixtures of ethylene oxide and said nonionic surfactant having a hydrophilelipophile balance greater than 10, and preferably greater than 12.
Detergent compositions according to the invention can also include other surfactants, for example anionic or zwitterionic surfactants, builders and other conventional detergent additives.
Detailed Description of the Invention Binary Active System Compositions of the present invention comprise, in combination, two essential ingredients, a monoglyceryl ether and an ethoxylated nonionic surfactant, which together form a binary active system affording excellent oily stain removal characteristics.
While not intending to be limited by theory, it is postulated that the linearity and the relatively strong intermolecular hydrogen bonding afforded by the hydrophilic, compact vicinal diol end group of the monoglyceryl ether result in enhanced grease/oil removal through the reduction of oil-water interfacialtension. The presence of the nonionic surfactant serves in part to solubilize the monoglyceryl ether so that it can reach the oil-water interface from aqueous solution and in part to assist in the removal of an oily stain. It is important that the nonionic surfactant be carefully selected so that it is fully compatible with the glyceryl ether. For example, nonionic surfactants having highly branched hydrophobic groups tend not to pack well at an oil/water interface with the glyceryl ether. It is therefore desirable that the nonionic surfactant has a substantially linear chain.
The monoglyceryl ether of the present invention has the general formula
where R is a substantially linear alkyl or alkenyl moiety having from 8 to 16 carbon atoms.
Preferably, R is a C8-Cl2 alkyl moiety, most preferably decyl, undecyl, or dodecyl.
The monoglyceryl ethers of alkanols are known materials and can be prepared, for example, by the condensation of a higher alkanol with glycidol.
The alkyl monoglyceryl ethers are lipophilic in character and, especially at alkyl chain lengths above 10 carbon atoms in length, have insufficient water solubility to act as useful surfactants in aqueous solutions.
In combination with certain alkoxylated nonionic surfactants, however, the alkyl monoglyceryl ethers adsorb very effectively from aqueous solution at an oil-water interface.
The alkoxylated nonionic surfactants for use in the present invention are preferably based on a substantially straight-chain hydrocarbon moiety. As used herein the term "substantially straight chain" is defined as linear or having not more than 30% branching consisting of Cl-C3 side chains at the 2-position. The term "substantially straight chain" thus includes within its scope the chain structure of alcohols prepared by the oxo process, which conventionally have up to 25% of Cl-C3 side chains at the 2-position.
The alkoxylate moiety of the nonionic surfactant is preferably polyethylene oxide, but can also be mixtures of oxides of ethylene and propylene.
In every case, the balance between the hydrocarbon moiety and the alkoxylate moiety must be such that the hydrophiliclipophilic balance (HLB) is greater than 10 and preferably greater than 12.
Especially suitable nonionic surfactants are the condensation products of substantially straight chain aliphatic alcohols with ethylene oxide. Examples of such ethoxylated alcohols include the condensation product of about 10 moles of ethylene oxide condensed with 1 mole of myristyl alcohol, the condensation product of about 6 moles of ethylene oxide with 1 mole of coconut fatty alcohol where the coconut alcohol is a mixture of C10-C14 alkanols, and the condensation product of about 9 moles of ethylene oxide with 1 mole of the above-described coconut alcohol.
Highly preferred surfactants are those based on synthetic alcohols prepared by the oxo process. Such alcohols are mixtures of primary alcohols having up to 25% of the mixture with methyl branching at the carbon atom adjacent to the hydroxyl-substituted carbon atom. The ethoxylated alcohols marketed by The Shell Chemical Company under the trade names Neodol or Dobanol are of this type. Very highly preferred examples are the stripped (see below) condensation products of 7 moles of ethylene oxide with 1 mole of a Cl4-Cls alcohol (Neodol 45-7), 8 moles of ethylene oxide with 1 mole of a C9-Cll alcohol (Dobanol 91-8) and 6.5 moles of ethylene oxide with 1 mole of a C12-C13 alcohol (Neodol 23-6.5).
Other useful surfactants are based on the secondary alcohols marketed by The Union Carbide Corporation under the trade name Tergitol. Tergitol 15-S-9, a condensation product of 9 moles of ethylene oxide with an average C15 alcohol, is a suitable example.
For best results, it is preferred that the ethoxylated alcohol is "stripped", i.e., is made substantially free of unethoxylated alcohol and low ethoxylate materials. It will be understood that the normal base-catalyzed ethoxylation process tends to produce a widely distributed range of ethoxylates averaging out at the derived product. The stripped ethoxylates have a relatively narrow distribution of ethoxylate content. In the present specification, the term "stripped condensation product of 7 moles of ethylene oxide with 1 mole of a Cl4-Cl5 alcohol," for example, means the product formed by ethoxylating 1 mole of C14-C15 alcohol with 7 moles of ethylene oxide and subsequently removing substantially all of the unethoxylated alcohol and the low ethoxylates (e.g., mono- and di- ethoxylates).
The ratio of nonionic surfactant to monoglyceryl ether can be varied over a wide range of from 4:1 to 1:4. Highly preferred embodiments are those where the ratio is from 4:1 to 1:1, especially 7:3 to 1:1.
The binary surfactant system of the present invention can be used as the sole surfactant system of a detergent composition, in which case the composition can include conventional ingredients of detergent compositions, such as builders, bleaches, anti-redeposition agents and enzymes. Such detergent compositions have particular utility for removal of greasy and oily stains.
The binary surfactant system can also be combined with co-surfactants, for example anionic or zwitterionic surfactants, or non-ethoxylated nonionic surfactants to provide detergent compositions having an oil soil removal benefit.
Co-surfactants Co-surfactants useful in detergent compositions of the present invention are selected from anionic, non-ethoxylated nonionic, zwitterionic and ampholytic surfactants. Most useful compositions are obtained when the binary nonionic system is combined with anionic or zwitterionic surfactants.
The ratio of co-surfactant:binary nonionic system can range from 10:1 to 1:10, preferably 4:1 to 1:1, especially about 2:1.
Examples of the above types of co-surfactants are listed in US Patent No. 3,862,058 of Nirschl and Gloss, the disclosure of which is incorporated herein by reference.
Particularly useful anionic surfactants include C8-C18 alkyl sulfates and sulfonates; (C9-C20 alkyl) benzene sulfonates, especially sodium or alkanolamine salts of linear straight chain alkyl benzene sulfonates in which the average chain length of the alkyl group is from 10 to 14, especially 11.8 carbon atoms (normally abbreviated NaCil.sLAS); alkyl ether sulfates of the formula RO(C2H40)n SO3M wherein R is CIo-C20 alkyl or alkenyl, n is 1-30 and M is an alkali metal cation; and olefin sulfonates derived by the sulfonation of C12-C24 a-olefins with sulfur trioxide.
While the binary surfactant system of the present invention can offer an oily soil removal benefit when combined with any anionic surfactant, especially efficacious compositions for combating grease and oil stains are provided by combining the binary surfactant system with alkaline earth metal preferably magnesium or calcium, salts of linear alkyl benzene sulfonic acid. The preferred material for this purpose is Mg(Cl1.4LAS)2. Ratios of MG(LAS)2:binary nonionic system from 4:1 to 1:1, preferably about 2:1, are especially useful.
Nonionic surfactants are less useful in conjunction with the binary system which itself contains a specific type of nonionic surfactant. However, non-ethoxylate-containing materials such as amine oxides, phosphine oxides and sulfoxides may be used in this context.
Specific examples of such surfactants include dimethyldodecylamine oxide, dimethylstearylamine oxide, bis-(2-hydroxyethyl) dodecylamine oxide, dimethyldodecylphosphine oxide, dodecylmethyl sulfoxide and octadecyl methyl sulfoxide.
Preferred zwitterionic surfactants include higher alkyl or alkaryl ammonio propane sulfonates, such as 3-(N,N-dimethyl- N-hexadecylammonio) propane -1-sulfonate, 3 (N,N-dimethhyl-N- hexadecylammonio)-2-hydroxy propane-1-sulfonate and 3 (N,N-dimethyl- N-alkylammonio-2-hydroxy propane-1-sulfonate, the alkyl group being devised from middle cut coconut fattyalcohbl,8nd higher alkyl or alkaryl ammoniocarboxylates such as (N-dodecylbenzyl-N, N-dimethyl ammonio) acetate, (N,N-dimethyl N-hexadecylammonio) acetate and 6-(N-dodecylbenzyl-N, N-dimethylammonio) hexanoate. Other useful zwitterionic materials are the ethoxylated ammonio-sulfonates and sulfates disclosed in US Patent Specification 3,929,678.
Builder Salts Detergent compositions of the present invention preferably include builder salts, especially alkaline, poly-valent anionic builder salts. These alkaline salts serve to maintain the pH of the laundry solution in the range from 7 to 12, preferably from 8 to 11.
Suitable detergent builder salts useful herein can be of the poly-valent inorganic or poly-valent organic types, or mixtures thereof. Non-limiting examples of suitable watersoluble, inorganic alkaline detergent builder salts include the alkali metal carbonates, borates, phosphates, polyphosphates, bicarbonates, silicates and sulfates. Specific examples of such salts include the sodium and potassium tetraborates, perborates, bicarbonates, carbonates, tripolyphosphates, orthophosphates and hexametaphosphates.
Examples of suitable organic alkaline detergency builder salts are: (1) water-soluble amino polyacetates, e.g., sodium and potassium ethylenediamine tetraacetates, nitrilotriacetates and N-(2-hydroxyethyl) nitrilodiacetates; (2) water-soluble salts of phytic acid, e.g., sodium and potassium phytates; (3) water-soluble polyphosphonates, including, sodium, potassium and lithium salts of ethane-1-hydroxy-1, 1-diphosphonic acid; sodium, potassium and lithium salts of methylenediphosphonic acid.
Additional organic builder salts useful herein include the polycarboxylate materials described in US Patent No. 2,264,103, including the water-soluble alkali metal salts of mellitic acid. The water-soluble salts of polycarboxylate polymers and copolymers such as are described in US Patent No. 3,308,067, incorporated herein by reference, are also suitable herein. It is to be understood that while the alkali metal salts of the foregoing inorganic and organic poly-valent anionic builder salts are preferred for use herein from an economic standpoint, the ammonium, alkanolammonium, e.g., triethanolammonium and diethanolammonium, water-soluble salts of any of the foregoing builder anions are useful herein.
Mixtures of organic and/or inorganic builders can be used herein. One such mixture of builders is disclosed in Canadian Patent No. 755,038, e.g. a ternary mixture of sodium tripolyphosphate, trisodium nitrilotriacetate and trisodium ethane-1-hydroxy-1, 1-diphosphonate.
While any of the foregoing alkaline poly-valent builder materials are useful herein, sodium tripolyphosphate, sodium nitrilotriacetate, sodium mellitate, sodium citrate and sodium carbonate are preferred herein for this builder use. Sodium tripolyphosphate is especially preferred herein as a builder both by virtue of its detergency builder activity and its ability to suspend illite and kaolinite clay soils and retarding their redeposition on the fabric surface.
Another type of detergency builder material useful in the present composition comprises a water-soluble material capable of forming a water-insoluble reaction product with water hardness cations in combination with a crystallization seed which is capable of providing growth sites for said reaction product. Such "seeded builder" compositions are fully disclosed in Belgian Patent No. 798, 856, issued October 29, 1973, the disclosure of which is incorporated herein by reference.
Specific examples of materials capable of forming the water-insoluble reaction product include the water-soluble salts of carbonates, bicarbonates, sesquicarbonates, silicates, aluminates, and oxalates. The alkali metal, especially sodium, salts of the foregoing materials are preferred for convenience and economy.
Another type of builder useful herein included various substantially water-insoluble materials which are capable of reducing the hardness content of laundering liquors, e.g., by ion-exchange processes. Examples of such builder materials include the phosphorylated cloths disclosed in U.S. Patent 3,424,545, inventor Bauman, issued January 28, 1969, incorporated herein by reference.
The complex aluminosilicates, i.e., zeolite-type materials, are useful presoaking/washing adjuvants herein in that these materials soften water, i.e., remove Ca++ hardness. Both the naturally occurring and synthetic "zeolites", especially zeolite A and hydrated zeolite A materials, are useful for this builder/ softener purpose. A description of zeolite materials and a method of preparation appears in Milton, U.S. Patent 2,882,243. British Patent Specification 1,424,406 describes the use of hydrated synthetic zeolites as builders.
The detergent builders are used at concentrations of from 10 percent to 60 percent, preferably 20 percent to 50 percent, by weight of the detergent compositions of this invention.
Other Components In addition to the above-described surfactant or builder components, the present compositions can optionally contain a wide variety of other conventional detergency adjuncts.
Representative materials of this type include, for example, the various anticaking agents, filler materials, soil suspending agents and as carboxymethylcellulose, anti-spotting agents, dyes, perfumes, suds boosters, suds depressants. These adjunct materials are commonly used as minor components (e.g., 0.1% to 5% wt.) in compositions of the present type.
Highly preferred optional additives herein include various bleaches commonly employed in presoak, laundry additive and detergent compositions. Such bleaches can include, for example, the various organic peroxyacids such as peradipic acid, perphthalic acid, diperphthalic acid and diperazelaic acid. Inorganic bleaches, i.e., persalts including such materials as sodium perborate, sodium perborate tetrahydrate and urea peroxide can be employed in the compositions herein. Bleaches are commonly used in the instant granular compositions at a level of from 1% to 45% by weight.
An especially preferred bleaching agent for use herein is sodium perborate tetrahydrate, at an effective concentration of from 10% to 30% by weight of the total composition.
Liquid or pasty compositions, in particular, can include materials to impart alkalinity to the detergent solution; typical of such materials are mono-, di- and tri-ethanolamine.
Various detergency enzymes well known in the art for their ability to degrade and aid in the removal of various soils and stains can also be employed in the present granular compositions.
Detergency enzymes are commonly used at concentrations of from 0.1 to 1.0% by weight of such compositions. Typical enzymes include the various proteases, lipases, amylases, and mixtures thereof, which are designed to remove a variety of soils and stains from fabrics.
Composition Preparation Compositions of the present invention can be prepared in any of a wide variety of product forms, for example as granules, powder, liquid, gel, paste or tablets. Where a solid product form is desired, a granular composition is generally preferred and slurry comprising a builder salt such as sodium tripolyphosphate and the surfactant system can be spray-dried to form granules. Alternatively, the product may be agglomerated, and this is preferred with certain nonionic surfactants which are relatively low-boiling and may degrade during spray drying.
In especially preferred compositions, the product is prepared in liquid form. Liquid products are very useful for grease removal as they can be used neat as a pre-treatment for oily stains. In liquid formulations, the surfactant mixture is normally dissolved in water or a water-alcohol mixture, preferred alcohols being C1-C3 alkanols, especially ethanol. In liquid formulations, particularly preferred co-surfactants are the magnesium calcium, triethanolammonium and monoethanolammonium salts of LAS.
Generally, the total surfactant level in compositions of the present invention ranges from 2% to 95 % by weight. Surfactant levels tend to be relatively high, from 30%to 50%, in liquid compositions and relatively low, from 10% to 20%, in granular compositions. Lower surfactant concentrations, for example from 2% to 10%, can be useful when the composition is designed for use without dilution. Compositions in the form of pastes or gels can have very high surfactant concentrations, up to 95%.
Performance Testing The oily stain removal performance of the binary active mixture of the present invention was tested by comparison with a single nonionic surfactant.
Cotton fabric cloths were artificially stained with a grease/oil stain and the cloths were washed in water of 7 grain hardness at 100"F in the presence of 300 ppm of surfactant. The control surfactant in all cases was Neodol 45-7, a condensate of 7 moles of ethylene oxide with one mole of a C14-C15 alcohol. The cloths, afterwashing, were visually graded by apanel of judges and the percentage stain removal was estimated.
In the results detailed below, the improvement in percentage stain removal over the control is recorded.
(a) Ratio of nonionic:alkyl glyceryl ether % Stripped % C10 Alkyl % Stain Removal Dobanol 91-8 Glyceryl Ether Improvement 90 10 -3 75 25 +12 60 40 +19 50 50 +18 (b) Type of Nonionic Binary mixtures of 60% nonionic surfactant and 40% of C10 alkyl glyceryl ether were tested.
Nonionic HLB % Stain Removal (approx.) Improvement Dobanol91-12 16 +11.5 Stripped Dobanol 91-8 14 +16 Neodol45-7 12 +11 Neodol23-3 10 +10 (c) Chain length of alkyl glyceryl ether Binary mixtures of 60% of stripped Dobanol 91- and 40% of various chain length alkyl glyceryl ethers were tested.
Chain Length % Stain Removal Improvement C8 - 3 C8.5 +4 Cg +4 Clo +19 C8-10 +9 C9-11 +16 The following examples illustrate compositions of the present invention.
Example I Granular detergent compositions were prepared having the following formulae: Compositions (wt. %) A B Stripped Dobanol 91-8 9.0 5.5 C10 alkyl glyceryl ether 9.0 5.5 Sodium carbonate 10.0 10.0 Sodium silicate (1.6 ratio SiO2:Na2O) 10.0 8.0 Sodium tripolyphosphate 24.4 32.0 Bentonite 6.0 5.0 Sodium sulfate 25.0 24.0 Moisture and minors to 100 to 100 The above compositions A and B were tested for soil removal by comparison with compositions identical except for the replacement of the binary active mixture by the same amount of a single nonionic surfactant (stripped Neodol 23-3).
The exemplified compositions were significantly better in their removal of greasy and oily stains and were not significantly different in their removal of clay soil.
Example II Compositions (wt. %)- A B C D Mg (Cl 1.4LAS)2 30 30 Monoethanolammonium Cl lALA5 18 18 Stripped Dobanol 91-8 10 22 Condensate product of 9 moles of ethylene oxide with 1 mole of a C13-C14 secondary alcohol 10 22 C10 alkyl glyceryl ether 5 11 C9-11 alkyl glyceryl ether 5 11 Triethanolamine 3 3 Monoethanolamine 2 2 Oleic acid 2 2 1 1 Ethanol 5 5 5 5 Water and minors ----to 100 ------------ The above heavy-duty liquid detergent compositions provided effective oily stain removal when used as a main wash detergent.
WHAT WE CLAIM IS: 1. A detergent composition comprising a binary surfactant system consisting of (a) from 80% to 20% by weight of monoglyceryl ether of the general formula
wherein R is a substantially linear alkyl or alkenyl moiety having from 8 to 16 carbon atoms, and (b) from 20% to 80% by weight of a nonionic surfactant which is a condensation product of a C9-C15 alcohol with an alkylene oxide selected from ethylene oxide and mixtures of ethylene oxide and propylene oxide, said nonionic surfactant having a hydrophile lipophile balance greater than 10.
2. A composition according to Claim 1 wherein R is C8-C12 alkyl.
3. A composition according to Claim 1 wherein the nonionic surfactant is a condensation product of ethylene oxide with a substantially straight chain aliphatic alcohol.
4. A composition according to Claim 3 wherein the ratio of the monoglyceryl ether to the nonionic surfactant is from 1:4 to 1:1.
5. A composition according to Claim 4 wherein said ratio is from 3:7 to 1:1.
6. A composition according to Claim 5 wherein the hydrophilic-lipophilic balance of the nonionic surfactant is greater than 12.
7. A composition according to Claim 6 wherein the nonionic surfactant is selected from the stripped condensation products of 7 moles of ethylene oxide with 1 mole of a C14-C1s
**WARNING** end of DESC field may overlap start of CLMS **.

Claims (21)

  1. **WARNING** start of CLMS field may overlap end of DESC **.
    The above compositions A and B were tested for soil removal by comparison with compositions identical except for the replacement of the binary active mixture by the same amount of a single nonionic surfactant (stripped Neodol 23-3).
    The exemplified compositions were significantly better in their removal of greasy and oily stains and were not significantly different in their removal of clay soil.
    Example II Compositions (wt. %)- A B C D Mg (Cl 1.4LAS)2 30 30 Monoethanolammonium Cl lALA5 18 18 Stripped Dobanol 91-8 10 22 Condensate product of
    9 moles of ethylene oxide with 1 mole of a C13-C14 secondary alcohol 10 22 C10 alkyl glyceryl ether 5 11 C9-11 alkyl glyceryl ether 5 11 Triethanolamine 3 3 Monoethanolamine 2 2 Oleic acid 2 2 1 1 Ethanol 5 5 5 5 Water and minors ----to 100 ------------ The above heavy-duty liquid detergent compositions provided effective oily stain removal when used as a main wash detergent.
    WHAT WE CLAIM IS: 1. A detergent composition comprising a binary surfactant system consisting of (a) from 80% to 20% by weight of monoglyceryl ether of the general formula
    wherein R is a substantially linear alkyl or alkenyl moiety having from 8 to 16 carbon atoms, and (b) from 20% to 80% by weight of a nonionic surfactant which is a condensation product of a C9-C15 alcohol with an alkylene oxide selected from ethylene oxide and mixtures of ethylene oxide and propylene oxide, said nonionic surfactant having a hydrophile lipophile balance greater than 10.
  2. 2. A composition according to Claim 1 wherein R is C8-C12 alkyl.
  3. 3. A composition according to Claim 1 wherein the nonionic surfactant is a condensation product of ethylene oxide with a substantially straight chain aliphatic alcohol.
  4. 4. A composition according to Claim 3 wherein the ratio of the monoglyceryl ether to the nonionic surfactant is from 1:4 to 1:1.
  5. 5. A composition according to Claim 4 wherein said ratio is from 3:7 to 1:1.
  6. 6. A composition according to Claim 5 wherein the hydrophilic-lipophilic balance of the nonionic surfactant is greater than 12.
  7. 7. A composition according to Claim 6 wherein the nonionic surfactant is selected from the stripped condensation products of 7 moles of ethylene oxide with 1 mole of a C14-C1s
    alkanol, of 8 moles of ethylene oxide with 1 mole of a C9-Cll alkanol and of 6.5 moles of ethylene oxide with 1 mole of a CirCi3 alkanol.
  8. 8. A composition according to Claim 6 wherein the R group of the monoglyceryl ether is C8-C12 alkyl.
  9. 9. A composition according to Claim 1 additionally comprising from 10% to 60% of a detergency builder.
  10. 10. A detergent composition comprising (a) a binary surfactant sytem consisting of (i) from 80% to 20% by weight of monoglyceryl ether of the general formula
    wherein R is a substantially linear alkyl or alkenyl moiety having from 7 to 16 carbon atoms, and (ii) from 20% to 80% by weight of a nonionic surfactant which is a condensation product of a C9-C1s alcohol with an alkylene oxide selected from ethylene oxide, propylene oxide and mixtures thereof, said condensation product having a hydrophile-lipophile balance greater than 10.
    and, (b) a co-surfactant selected from anionic, non-ethoxylated nonionic, ampholytic and zwitterionic surfactants, the ratio of (a) to (b) being from 10:1 to 1:10.
  11. 11. A composition according to Claim 10 wherein the ratio of (a) to (b) is from 1:4 to 1:1.
  12. 12. A composition according to Claim 11 wherein the nonionic surfactant of the binary surfactant system is a condensation product of ethylene oxide with a substantially straight chain aliphatic alcohol and has a hydrophile-lipophile balance of greater than 12.
  13. 13. A composition according to Claim 12 wherein the ratio of the monoglyceryl ether to the nonionic surfactant in the binary surfactant system is from 1:4 to 1:1.
  14. 14. A composition according to Claim 13 wherein the R group of the monoglyceryl ether is C8-C12 alkyl.
  15. 15. A composition according to Claim 10 wherein the co-surfactant is selected from the group consisting of alkali metal ammonium and alkanolammonium salts of (C9-C20 alkyl) benzene sulfonic acid, C8-Cl8 alkyl sulfonates, C8-C18 alkyl sulfates, olefin sulfonates derived from C12-C24 a-olefins and (C,0-C20 alkyl) ether sulfates.
  16. 16. A composition according to Claim 10 wherein the co-surfactant is selected from the group consisting of calcium and magnesium salts of alkyl benzene sulfonic acid having from 10 to 14 carbon atoms in the alkyl chain.
  17. 17. A composition according to Claim 16 wherein the ratio of (a) to (b) is from 1:4 to 1:1.
  18. 18. A composition according to Claim 17 wherein the ratio of the monoglyceryl ether to the nonionic surfactant in the binary surfactant system is from 1:4 to 1:1.
  19. 19. A composition according to Claim 18 wherein the nonionic surfactant is selected from the stripped condensation products of 7 moles of ethylene oxide with 1 mole of a Cl4-Cls alkanol, of 8 moles of ethylene oxide with 1 mole of a C9-Cll alkanol and of 6.5 moles of ethylene oxide with 1 mole of a CirCi3 alkanol.
  20. 20. A composition according to Claim 19 wherein the ratio of (a) to (b) is about 1:2.
  21. 21. A composition according to Claim 1, as hereinbefore specifically identified.
GB5351976A 1975-12-24 1976-12-22 Detergent compositions Expired GB1560083A (en)

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GB5351976A Expired GB1560083A (en) 1975-12-24 1976-12-22 Detergent compositions

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JP (1) JPS52101211A (en)
BE (1) BE849807A (en)
CA (1) CA1081574A (en)
DE (1) DE2657517A1 (en)
FR (1) FR2336474A1 (en)
GB (1) GB1560083A (en)
IT (1) IT1065503B (en)
NL (1) NL184911C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6417146B1 (en) 1999-10-12 2002-07-09 Kao Corporation Aqueous liquid detergent compositions having a surfactant, fatty acid glycol ester and a glyceryl ether

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Publication number Priority date Publication date Assignee Title
US4217296A (en) * 1978-07-24 1980-08-12 Fmc Corporation Alkyl glyceryl ether sulfate salts and process for their preparation
US4269786A (en) * 1978-11-13 1981-05-26 Fmc Corporation Alkyl glyceryl ether sulfate salts and process for their preparation
US4298764A (en) * 1979-07-27 1981-11-03 Fmc Corporation Preparation of alkyl glyceryl ether alcohols
US4430237A (en) * 1981-10-16 1984-02-07 Colgate-Palmolive Co. Liquid detergent having high grease removal ability
GB8914602D0 (en) * 1989-06-26 1989-08-16 Unilever Plc Liquid detergent composition
JP3645455B2 (en) * 1999-09-06 2005-05-11 花王株式会社 Cleaning composition

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US2900346A (en) * 1956-02-20 1959-08-18 Shell Dev Foaming detergent compositions
US3666671A (en) * 1965-04-23 1972-05-30 Oreal Detergent composition and process of shampooing hair therewith
US3427248A (en) * 1965-10-22 1969-02-11 Lever Brothers Ltd Detergent
US3558499A (en) * 1969-07-01 1971-01-26 Atlas Chem Ind Anti-redeposition agents

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6417146B1 (en) 1999-10-12 2002-07-09 Kao Corporation Aqueous liquid detergent compositions having a surfactant, fatty acid glycol ester and a glyceryl ether

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BE849807A (en) 1977-06-23
FR2336474A1 (en) 1977-07-22
NL184911C (en) 1989-12-01
IT1065503B (en) 1985-02-25
NL184911B (en) 1989-07-03
CA1081574A (en) 1980-07-15
DE2657517A1 (en) 1977-07-07
FR2336474B1 (en) 1980-07-18
NL7614390A (en) 1977-06-28
DE2657517C2 (en) 1987-12-17
JPS52101211A (en) 1977-08-25

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Effective date: 19961221